Factors influencing place of death and disenrollment among patients receiving specialist palliative care

Factors influencing place of death and disenrollment among patients receiving specialist palliative care

Authors

  • Marco Di Nitto Department of biomedicine and prevention, University of Rome “Tor Vergata”, Rome, Italy
  • Marco Artico Department of Palliative Care and Pain Therapy Unit, Azienda ULSS n.4 Veneto Orientale, San Donà di Piave, Italy
  • Michela Piredda Research Unit Nursing Science, Campus Bio-Medico di Roma University, Rome, Italy
  • Maddalena De Maria Department of biomedicine and prevention, University of Rome “Tor Vergata”, Rome, Italy
  • Caterina Magnani Local health unit Roma 1, Rome, Italy
  • Anna Marchetti Research Unit Nursing Science, Campus Bio-Medico di Roma University, Rome, Italy
  • Chiara Mastroianni Fondazione Campus Bio-Medico, Rome, Italy
  • Roberto Latina Deptment of Health Promotion Sciences, Maternal & Infant Care, Internal Medicine & Excellence Specialists University of Palermo, Palermo, Italy
  • Maria Grazia De Marinis Research Unit Nursing Science, Campus Bio-Medico di Roma University, Rome, Italy
  • Daniela D'Angelo National Institute of Health, Rome, Italy

Keywords:

Andersen’s behavioural model of health services use, place of death, patient discharge, palliative care, facilities and services utilization, logistic models, retrospective studies

Abstract

Background and aim of the work: Place of death and disenrollment from specialized palliative care services (SPCSs) are two aspects that determine service utilization. These aspects should be determined by patient needs and preferences, but they are often associated to patient sociodemographic or contextual characteristics. The aim of this study was to describe which factors are associated with utilizing SPCSs in terms of place of death and disenrollment.

Methods: Retrospective cohort study. Patients (>18 years) who died or were disenrolled during SPCSs utilization. Two hierarchical regression models were performed, and variables were categorized in predisposing, enabling, and need factors according to the Andersen behavioral model of health services use.

Results: We included 35,869 patients (52,5% male, mean age 74,6 ± 12,3 SD), where 17,225 patients died in hospice and 16,953 at home, while 1,691 patients were disenrolled. Dying at home was associated with older age, oncological diagnosis, painful symptoms and longer survival time. Instead, service disenrollment was associated with less education, longer wait time and longer length of stay.

Conclusions: SPCS utilization was not influenced only by patient need, but also by other factors, such as social and contextual factors. These factors need to be considered by health care providers and efforts are needed for 1) identifying barriers and implementing effective interventions to support patients and caregivers in their preferred place of care and death and 2) for avoiding SPCS disenrollment with an increased probability of aggressive treatments and worse quality of life for patients.

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Published

12-05-2022

How to Cite

1.
Di Nitto M, Artico M, Piredda M, De Maria M, Magnani C, Marchetti A, et al. Factors influencing place of death and disenrollment among patients receiving specialist palliative care. Acta Biomed [Internet]. 2022 May 12 [cited 2024 Jul. 18];93(S2):e2022189. Available from: https://mattioli1885journals.com/index.php/actabiomedica/article/view/12637